A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155366



Internal ID15875630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90561197..90592034hg38UCSC Ensembl
Innerchr7:90190511..90221348hg19UCSC Ensembl
Innerchr7:90028447..90059284hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3830838
hg1930838
hg1830838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607792
Supporting Variants
SamplesHGDP00711
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155366
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer